Polyakova, Lydia A.

Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors

Gordeuk, V. R., Sergueeva, A. I., Miasnikova, G. Y., Okhotin, D., Voloshin, Y., Choyke, P. L., Butman, J. A., Jedlickova, K., Prchal, J. T., & Polyakova, L. A. (2004) · Blood

Erythropoietin and Anemia TreatmentCancer, Hypoxia, and Metabolism

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Endemic Polycythemia in Russia: Mutation in the VHL Gene

Ang, S. O., Chen, H., Gordeuk, V. R., Sergueeva, A. I., Polyakova, L. A., Miasnikova, G. Y., Kralovics, R., Stockton, D. W., & Prchal, J. T. (2002) · Blood Cells, Molecules, and Diseases

Erythropoietin and Anemia TreatmentHemoglobinopathies and Related Disorders

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The worldwide distribution of the VHL 598C>T mutation indicates a single founding event

Liu, E., Percy, M. J., Amos, C. I., Guan, Y., Shete, S., Stockton, D. W., McMullin, M. F., Polyakova, L. A., Ang, S. O., Pastore, Y. D., et al. (2004) · Blood

Genetic Associations and EpidemiologyForensic and Genetic Research

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Chuvash polycythemia VHLR200W mutation is associated with down-regulation of hepcidin expression

Gordeuk, V. R., Miasnikova, G. Y., Sergueeva, A. I., Niu, X., Nouraie, M., Okhotin, D. J., Polyakova, L. A., Ammosova, T., Nekhai, S., Ganz, T., et al. (2011) · Blood

Iron Metabolism and DisordersErythropoietin and Anemia Treatment

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